RU2010111142A - SELF-RESTRICTED CATALYTIC SYSTEM WITH AN ADJUSTABLE RATIO OF ALUMINUM AND SCA AND METHOD - Google Patents

SELF-RESTRICTED CATALYTIC SYSTEM WITH AN ADJUSTABLE RATIO OF ALUMINUM AND SCA AND METHOD Download PDF

Info

Publication number
RU2010111142A
RU2010111142A RU2010111142/04A RU2010111142A RU2010111142A RU 2010111142 A RU2010111142 A RU 2010111142A RU 2010111142/04 A RU2010111142/04 A RU 2010111142/04A RU 2010111142 A RU2010111142 A RU 2010111142A RU 2010111142 A RU2010111142 A RU 2010111142A
Authority
RU
Russia
Prior art keywords
composition
sca
aluminum
catalytic composition
composition according
Prior art date
Application number
RU2010111142/04A
Other languages
Russian (ru)
Other versions
RU2470947C2 (en
Inventor
Линьфэн ЧЭНЬ (US)
Линьфэн ЧЭНЬ
Ричард Э. КЭМПБЕЛЛ (US)
Ричард Э. КЭМПБЕЛЛ
ЭГМОНД Ян В. ВАН (US)
ЭГМОНД Ян В. ВАН
Original Assignee
Дау Глобал Текнолоджиз, Инк. (Us)
Дау Глобал Текнолоджиз, Инк.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=39768748&utm_source=***_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=RU2010111142(A) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Дау Глобал Текнолоджиз, Инк. (Us), Дау Глобал Текнолоджиз, Инк. filed Critical Дау Глобал Текнолоджиз, Инк. (Us)
Publication of RU2010111142A publication Critical patent/RU2010111142A/en
Application granted granted Critical
Publication of RU2470947C2 publication Critical patent/RU2470947C2/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F4/00Polymerisation catalysts
    • C08F4/42Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors
    • C08F4/44Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides
    • C08F4/60Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides together with refractory metals, iron group metals, platinum group metals, manganese, rhenium technetium or compounds thereof
    • C08F4/62Refractory metals or compounds thereof
    • C08F4/64Titanium, zirconium, hafnium or compounds thereof
    • C08F4/65Pretreating the metal or compound covered by group C08F4/64 before the final contacting with the metal or compound covered by group C08F4/44
    • C08F4/652Pretreating with metals or metal-containing compounds
    • C08F4/656Pretreating with metals or metal-containing compounds with silicon or compounds thereof
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F10/00Homopolymers and copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
    • C08F10/02Ethene
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/02Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J8/00Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes
    • B01J8/18Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with fluidised particles
    • B01J8/1809Controlling processes
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J8/00Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes
    • B01J8/18Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with fluidised particles
    • B01J8/1872Details of the fluidised bed reactor
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F10/00Homopolymers and copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
    • C08F10/04Monomers containing three or four carbon atoms
    • C08F10/06Propene
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F110/00Homopolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
    • C08F110/04Monomers containing three or four carbon atoms
    • C08F110/06Propene
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F4/00Polymerisation catalysts
    • C08F4/42Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors
    • C08F4/44Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides
    • C08F4/60Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides together with refractory metals, iron group metals, platinum group metals, manganese, rhenium technetium or compounds thereof
    • C08F4/62Refractory metals or compounds thereof
    • C08F4/64Titanium, zirconium, hafnium or compounds thereof
    • C08F4/646Catalysts comprising at least two different metals, in metallic form or as compounds thereof, in addition to the component covered by group C08F4/64
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/02Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
    • B01J31/0201Oxygen-containing compounds
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/02Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
    • B01J31/0201Oxygen-containing compounds
    • B01J31/0211Oxygen-containing compounds with a metal-oxygen link
    • B01J31/0212Alkoxylates
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/02Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
    • B01J31/0272Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing elements other than those covered by B01J31/0201 - B01J31/0255
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/02Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
    • B01J31/12Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing organo-metallic compounds or metal hydrides
    • B01J31/128Mixtures of organometallic compounds
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/02Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
    • B01J31/12Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing organo-metallic compounds or metal hydrides
    • B01J31/14Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing organo-metallic compounds or metal hydrides of aluminium or boron
    • B01J31/143Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing organo-metallic compounds or metal hydrides of aluminium or boron of aluminium
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/16Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • B01J31/22Organic complexes
    • B01J31/2204Organic complexes the ligands containing oxygen or sulfur as complexing atoms
    • B01J31/2208Oxygen, e.g. acetylacetonates
    • B01J31/2213At least two complexing oxygen atoms present in an at least bidentate or bridging ligand
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/16Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • B01J31/22Organic complexes
    • B01J31/2204Organic complexes the ligands containing oxygen or sulfur as complexing atoms
    • B01J31/2208Oxygen, e.g. acetylacetonates
    • B01J31/2226Anionic ligands, i.e. the overall ligand carries at least one formal negative charge
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F210/00Copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
    • C08F210/04Monomers containing three or four carbon atoms
    • C08F210/06Propene
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F2400/00Characteristics for processes of polymerization
    • C08F2400/02Control or adjustment of polymerization parameters

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Engineering & Computer Science (AREA)
  • Combustion & Propulsion (AREA)
  • Materials Engineering (AREA)
  • Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
  • Polymerisation Methods In General (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
  • Emergency Medicine (AREA)

Abstract

1. Каталитическая композиция, включающая: ! одну или несколько композиций прокатализатора Циглера-Натта, содержащих одно или несколько соединений переходных металлов и один или несколько внутренних доноров электронов в виде эфиров ароматической дикарбоновой кислоты; !один или несколько алюминийсодержащих сокатализаторов и агент для контроля за селективностью (SCA), включающий смесь эфира C4-C30-алифатической кислоты и силановой композиции, и молярное соотношение алюминия и суммарного SCA составляет от 0,5:1 до 4:1. ! 2. Каталитическая композиция по п.1, в которой молярное соотношение алюминия и суммарного SCA составляет от 1:1 до 3:1. ! 3. Каталитическая композиция по п.1, в которой эфир C4-C30-алифатической кислоты выбирают из группы, включающей: изопропилмиристат, ди-н-бутилсебацинат, (поли)(алкиленгликоль)-моно- или ди-миристаты и комбинации указанных соединений. ! 4. Каталитическая композиция по п.1, в которой силановая композиция представляет собой дициклопентилдиметоксисилан. !5. Каталитическая композиция по п.1, в которой силановая композиция представляет собой смесь диметилдиметоксисилана и члена, выбираемого из группы, включающей: дициклопентилдиметоксисилан, метилциклогексилдиметоксисилан и н-пропилтриметоксисилан. ! 6. Каталитическая композиция по п.1, в которой SCA содержит 60-97 мол.% сложного C4-C30-алифатического эфира и 3-40 мол.% силановой композиции. ! 7. Каталитическая композиция по п.1, включающая изопропилмиристат и дициклопентилдиметоксисилан. ! 8. Каталитическая композиция по п.1, включающая ди-н-бутилсебацинат и дициклопентилдиметоксисилан. ! 9. Каталитическая композиция по п.1, включающая алкиловый эфир C8-C30-алифат 1. The catalytic composition, including:! one or more Ziegler-Natta procatalyst compositions containing one or more transition metal compounds and one or more internal electron donors in the form of aromatic dicarboxylic acid esters; ! one or more aluminum-containing cocatalysts and a selectivity control agent (SCA) comprising a mixture of a C4-C30 aliphatic acid ester and a silane composition, and a molar ratio of aluminum to total SCA is from 0.5: 1 to 4: 1. ! 2. The catalyst composition according to claim 1, in which the molar ratio of aluminum to total SCA is from 1: 1 to 3: 1. ! 3. The catalytic composition according to claim 1, wherein the C4-C30 aliphatic acid ester is selected from the group consisting of: isopropyl myristate, di-n-butylsebacinate, (poly) (alkylene glycol) mono- or di-myristates and combinations of these compounds. ! 4. The catalytic composition according to claim 1, in which the silane composition is dicyclopentyldimethoxysilane. !5. The catalyst composition of claim 1, wherein the silane composition is a mixture of dimethyldimethoxysilane and a member selected from the group consisting of dicyclopentyldimethoxysilane, methylcyclohexyl dimethoxysilane and n-propyltrimethoxysilane. ! 6. The catalytic composition according to claim 1, in which the SCA contains 60-97 mol.% Complex C4-C30 aliphatic ester and 3-40 mol.% Silane composition. ! 7. The catalytic composition according to claim 1, including isopropyl myristate and dicyclopentyldimethoxysilane. ! 8. The catalytic composition according to claim 1, including di-n-butylsebacinate and dicyclopentyl dimethoxysilane. ! 9. The catalytic composition according to claim 1, comprising a C8-C30 aliphate alkyl ester

Claims (48)

1. Каталитическая композиция, включающая:1. The catalytic composition, including: одну или несколько композиций прокатализатора Циглера-Натта, содержащих одно или несколько соединений переходных металлов и один или несколько внутренних доноров электронов в виде эфиров ароматической дикарбоновой кислоты;one or more Ziegler-Natta procatalyst compositions containing one or more transition metal compounds and one or more internal electron donors in the form of aromatic dicarboxylic acid esters; один или несколько алюминийсодержащих сокатализаторов и агент для контроля за селективностью (SCA), включающий смесь эфира C4-C30-алифатической кислоты и силановой композиции, и молярное соотношение алюминия и суммарного SCA составляет от 0,5:1 до 4:1.one or more aluminum-containing cocatalysts and a selectivity control agent (SCA) comprising a mixture of a C 4 -C 30 aliphatic acid ester and a silane composition, and a molar ratio of aluminum to total SCA is from 0.5: 1 to 4: 1. 2. Каталитическая композиция по п.1, в которой молярное соотношение алюминия и суммарного SCA составляет от 1:1 до 3:1.2. The catalyst composition according to claim 1, in which the molar ratio of aluminum to total SCA is from 1: 1 to 3: 1. 3. Каталитическая композиция по п.1, в которой эфир C4-C30-алифатической кислоты выбирают из группы, включающей: изопропилмиристат, ди-н-бутилсебацинат, (поли)(алкиленгликоль)-моно- или ди-миристаты и комбинации указанных соединений.3. The catalytic composition according to claim 1, wherein the C 4 -C 30 aliphatic acid ester is selected from the group consisting of: isopropyl myristate, di-n-butyl sebacinate, (poly) (alkylene glycol) mono or di myristates, and combinations thereof compounds. 4. Каталитическая композиция по п.1, в которой силановая композиция представляет собой дициклопентилдиметоксисилан.4. The catalytic composition according to claim 1, in which the silane composition is dicyclopentyldimethoxysilane. 5. Каталитическая композиция по п.1, в которой силановая композиция представляет собой смесь диметилдиметоксисилана и члена, выбираемого из группы, включающей: дициклопентилдиметоксисилан, метилциклогексилдиметоксисилан и н-пропилтриметоксисилан.5. The catalytic composition according to claim 1, in which the silane composition is a mixture of dimethyldimethoxysilane and a member selected from the group consisting of: dicyclopentyldimethoxysilane, methylcyclohexyl dimethoxysilane and n-propyltrimethoxysilane. 6. Каталитическая композиция по п.1, в которой SCA содержит 60-97 мол.% сложного C4-C30-алифатического эфира и 3-40 мол.% силановой композиции.6. The catalytic composition according to claim 1, in which the SCA contains 60-97 mol.% Complex C 4 -C 30 aliphatic ester and 3-40 mol.% Silane composition. 7. Каталитическая композиция по п.1, включающая изопропилмиристат и дициклопентилдиметоксисилан.7. The catalytic composition according to claim 1, including isopropyl myristate and dicyclopentyldimethoxysilane. 8. Каталитическая композиция по п.1, включающая ди-н-бутилсебацинат и дициклопентилдиметоксисилан.8. The catalytic composition according to claim 1, including di-n-butylsebacinate and dicyclopentyl dimethoxysilane. 9. Каталитическая композиция по п.1, включающая алкиловый эфир C8-C30-алифатической кислоты, и полимер, полимер, получаемый с помощью каталитической композиции, не имеет запаха.9. The catalytic composition according to claim 1, comprising a C 8 -C 30 aliphatic acid alkyl ester, and the polymer, polymer obtained by the catalytic composition, is odorless. 10. Каталитическая композиция, включающая:10. The catalytic composition, including: одну или несколько композиций прокатализатора Циглера-Натта, содержащих одно или несколько соединений переходных металлов и один или несколько внутренних доноров электронов в виде эфиров ароматической дикарбоновой кислоты;one or more Ziegler-Natta procatalyst compositions containing one or more transition metal compounds and one or more internal electron donors in the form of aromatic dicarboxylic acid esters; один или несколько алюминий-содержащих сокатализаторов иone or more aluminum-containing cocatalysts and агент для контроля за селективностью (SCA), включающий смесь не содержащей сложный эфир композиции и силановой композиции.selectivity control agent (SCA) comprising a mixture of an ester-free composition and a silane composition. 11. Каталитическая композиция по п.10, в которой не содержащую сложный эфир композицию выбирают из группы, включающей: соединение простого диалкилового диэфира, поли(алкенгликоль) и простой моно- или ди-алкиловый эфир поли(алкенгликол)я.11. The catalyst composition of claim 10, wherein the ester-free composition is selected from the group consisting of: dialkyl diester compound, poly (alkylene glycol) and poly (alkene glycol) mono- or di-alkyl ether. 12. Каталитическая композиция по п.1, имеющая молярное соотношение алюминия и суммарного SCA в пределах от 0,5:1 до 50:1.12. The catalyst composition according to claim 1, having a molar ratio of aluminum to total SCA ranging from 0.5: 1 to 50: 1. 13. Каталитическая композиция по п.9, в которой не содержащая сложный эфир композиция представляет собой 2,2-диизобутил-1,3-диметоксипропан.13. The catalyst composition of claim 9, wherein the ester-free composition is 2,2-diisobutyl-1,3-dimethoxypropane. 14. Каталитическая композиция по п.9, в которой SCA дополнительно включает ограничивающий активность агент.14. The catalytic composition according to claim 9, in which the SCA further includes an activity limiting agent. 15. Каталитическая композиция по п.9, имеющая молярное соотношение алюминия и суммарного SCA в пределах от 0,5:1 до 4:1.15. The catalyst composition according to claim 9, having a molar ratio of aluminum to total SCA ranging from 0.5: 1 to 4: 1. 16. Каталитическая композиция, включающая:16. A catalytic composition comprising: одну или несколько композиций прокатализатора Циглера-Натта, содержащих одно или несколько соединений переходных металлов и один или несколько внутренних доноров электронов в виде эфиров ароматической дикарбоновой кислоты;one or more Ziegler-Natta procatalyst compositions containing one or more transition metal compounds and one or more internal electron donors in the form of aromatic dicarboxylic acid esters; один или несколько алюминийсодержащих сокатализаторов иone or more aluminum-containing cocatalysts and агент для контроля за селективностью (SCA), включающий смесь (i) силановой композиции из первого алкоксисилана и второго алкоксисилан и (ii) ограничивающего активность агента.selectivity control agent (SCA) comprising a mixture of (i) a silane composition from a first alkoxysilane and a second alkoxysilane and (ii) an activity limiting agent. 17. Каталитическая композиция по п.16, в которой первый алкоксисилан выбирают из группы, включающей: диметилдиметоксисилан, диизопропилдиметоксисилан, дициклопентилдиметоксисилан и бис(пергидроизохинолино)диметоксисилан.17. The catalytic composition according to clause 16, in which the first alkoxysilane is selected from the group consisting of: dimethyldimethoxysilane, diisopropyl dimethoxysilane, dicyclopentyl dimethoxysilane and bis (perhydroisoquinolino) dimethoxysilane. 18. Каталитическая композиция по п.16, в которой второй алкоксисилан выбирают из группы, включающей: диметилдиметоксисилан, этилтриэтоксисилан, н-пропилтриэтоксисилан, диизобутилдиэтоксисилан, метилциклогексилдиэтоксисилан, ди-н-бутилдиметоксисилан, тетраэтоксисилан и тетраметоксисилан.18. The catalytic composition according to clause 16, in which the second alkoxysilane is selected from the group comprising: dimethyldimethoxysilane, ethyltriethoxysilane, n-propyltriethoxysilane, methylcyclohexyl diethoxysilane, di-n-butyldimethoxysilane tetra. 19. Каталитическая композиция по п.16, в которой ограничивающий активность агент выбирают из группы, включающей: этил-п-этоксибензоат, C1-20-алкиловые эфиры алифатических C4-30-моно- или ди-карбоновых кислот и C4-20- моно- или поли-карбоксилатные производные C2-100-(поли)гликолей или простых C2-100-(поли)гликолевых эфиров.19. The catalytic composition according to clause 16, in which the activity-limiting agent is selected from the group consisting of: ethyl p-ethoxybenzoate, C 1-20- alkyl esters of aliphatic C 4-30 mono- or di-carboxylic acids and C 4- 20 - mono- or poly-carboxylate derivatives of C 2-100 - (poly) glycols or C 2-100 - (poly) glycol ethers. 20. Каталитическая композиция по п.16, в которой ограничивающий активность агент выбирают из группы, включающей: изопропиллаурат, изопропилмиристат и изопропилстеарат.20. The catalytic composition according to clause 16, in which the activity-limiting agent is selected from the group consisting of: isopropyl laurate, isopropyl myristate and isopropyl stearate. 21. Каталитическая композиция по п.16, в которой первый алкоксисилан представляет собой диметилдиметоксисилан и второй алкоксисилан выбирают из группы, включающей: дициклопентилдиметоксисилан, метилциклогексилдиметоксисилан и н-пропилтриметоксисилан.21. The catalyst composition of claim 16, wherein the first alkoxysilane is dimethyldimethoxysilane and the second alkoxysilane is selected from the group consisting of dicyclopentyldimethoxysilane, methylcyclohexyl dimethoxysilane and n-propyltrimethoxysilane. 22. Каталитическая композиция по п.16, имеющая молярное соотношение алюминия и суммарного SCA в пределах от 0,5:1 до 4:1.22. The catalyst composition according to clause 16, having a molar ratio of aluminum to total SCA in the range from 0.5: 1 to 4: 1. 23. Каталитическая композиция по п.16, в которой ограничивающий активность агент выбирают из группы, включающей: алкиловый эфир C4-C30-алифатической кислоты, простой диэфир и (поли)(алкиленгликолевый) эфир C4-C30-алифатической кислоты, и молярное соотношение алюминия и SCA составляет от 0,5:1 до 50:1.23. The catalytic composition according to clause 16, in which the activity limiting agent is selected from the group consisting of: C 4 -C 30 aliphatic acid alkyl ester, diester and ( 4 ) C 30 aliphatic acid poly (alkylene glycol) ester, and the molar ratio of aluminum to SCA is from 0.5: 1 to 50: 1. 24. Каталитическая композиция, включающая:24. A catalytic composition comprising: одну или несколько композиций прокатализатора Циглера-Натта, содержащих одно или несколько соединений переходных металлов и один или несколько внутренних доноров электронов в виде эфиров ароматической дикарбоновой кислоты;one or more Ziegler-Natta procatalyst compositions containing one or more transition metal compounds and one or more internal electron donors in the form of aromatic dicarboxylic acid esters; один или несколько алюминийсодержащих сокатализаторов иone or more aluminum-containing cocatalysts and агент для контроля за селективностью (SCA), включающий смесь (i) селективно ограничивающей композиции из алкоксисилана и несилановой композиции, и (ii) ограничивающего активность агента.a selectivity control agent (SCA) comprising a mixture of (i) a selectively limiting composition of an alkoxysilane and a non-silane composition, and (ii) an activity limiting agent. 25. Каталитическая композиция по п.24, в которой несилановую композицию выбирают из группы, включающей: соединения простого диэфира и пиперидиновые соединения.25. The catalytic composition according to paragraph 24, in which the non-silane composition is selected from the group including: diester compounds and piperidine compounds. 26. Каталитическая композиция по п.24, в которой несилановая композиция представляет собой 2,2-диизобутил-1,3-диметоксипропан.26. The catalytic composition according to paragraph 24, in which the non-silane composition is a 2,2-diisobutyl-1,3-dimethoxypropane. 27. Каталитическая композиция по п.24, в которой несилановая композиция представляет собой 2,2,6,6-тетраметилпиперидин.27. The catalytic composition according to paragraph 24, in which the non-silane composition is a 2,2,6,6-tetramethylpiperidine. 28. Способ полимеризации, включающий:28. The method of polymerization, including: введение пропилена и каталитической композиции в реактор-полимеризатор, каталитическая композиция включает композицию прокатализатора Циглера-Натта, внутренний донор электронов в виде эфира ароматической дикарбоновой кислоты, алюминийсодержащий сокатализатор и агент для контроля за селективностью (SCA), содержащий смесь ограничивающего активность агента и силановой композиции;introducing propylene and a catalyst composition into a polymerisation reactor, the catalyst composition includes a Ziegler-Natta procatalyst composition, an internal electron donor in the form of an aromatic dicarboxylic acid ester, an aluminum-containing cocatalyst, and a selectivity control agent (SCA) containing a mixture of an activity-limiting agent and a silane composition; обеспечение соотношения алюминия и суммарного SCA в пределах от 0,5:1 до 4:1 иensuring the ratio of aluminum and total SCA in the range from 0.5: 1 to 4: 1 and получение пропиленсодержащего полимера.obtaining a propylene-containing polymer. 29. Способ полимеризации по п.28, включающий введение в реактор SCA, содержащего смесь сложного C4-C30-алифатического эфира и силановой композиции.29. The polymerization process of claim 28, comprising introducing into the SCA reactor a mixture of a C 4 -C 30 aliphatic ester and a silane composition. 30. Способ полимеризации по п.28, включающий введение в реактор SCA, состоящего из не содержащей сложный эфир композиции и силановой композиции.30. The polymerization method according to p, comprising introducing into the SCA reactor, consisting of an ester-free composition and a silane composition. 31. Способ полимеризации по п.28, включающий введение в реактор SCA, состоящего из смеси (i) первого алкоксисилана и второго алкоксисилана и (ii) ограничивающего активность агента.31. The polymerization process of claim 28, comprising introducing into the SCA reactor a mixture of (i) a first alkoxysilane and a second alkoxysilane and (ii) an activity limiting agent. 32. Способ полимеризации по п.28, включающий поддержание соотношения алюминий и титан приблизительно при 45:1.32. The polymerization method according to p, including maintaining the ratio of aluminum and titanium at approximately 45: 1. 33. Способ полимеризации по п.28, по которому пропиленсодержащий полимер имеет содержание растворимых в ксилоле веществ приблизительно от 0,5 до 6,0 мас.%.33. The polymerization method according to p, in which the propylene-containing polymer has a content of soluble in xylene substances from about 0.5 to 6.0 wt.%. 34. Способ по п.28, включающий гашение с помощью каталитической композиции процесса полимеризации, когда реактор-полимеризатор имеет температуру свыше 100°C.34. The method according to p. 28, including quenching using a catalytic composition of the polymerization process, when the polymerization reactor has a temperature above 100 ° C. 35. Способ полимеризации, включающий:35. The method of polymerization, including: введение газа, содержащего пропилен и каталитическую композицию, в реактор-полимеризатор, каталитическая композиция включает композицию прокатализатора Циглера-Натта, внутренний донор электронов, алюминийсодержащий сокатализатор и агент для контроля за селективностью (SCA), содержащий смесь ограничивающего активность агента и силановой композиции;introducing a gas containing propylene and a catalyst composition into a polymerization reactor, the catalyst composition includes a Ziegler-Natta procatalyst composition, an internal electron donor, an aluminum-containing cocatalyst, and a selectivity control agent (SCA) containing a mixture of an activity-limiting agent and a silane composition; формирование псевдоожиженного слоя полимерных частиц, создание объемной плотности псевдоожиженного слоя; иthe formation of a fluidized bed of polymer particles, the creation of bulk density of the fluidized bed; and снижение парциального давления пропилена с целью повышения объемной плотности без загрязнения реактора.reduction of the partial pressure of propylene in order to increase bulk density without contaminating the reactor. 36. Способ по п.35, включающий увеличение объемной плотности на величину приблизительно от 10 до 100%.36. The method according to clause 35, comprising increasing the bulk density by a value of from about 10 to 100%. 37. Способ по п.35, включающий поддержание соотношения алюминия и суммарного SCA приблизительно в пределах от 0,5:1 до 4:1.37. The method according to clause 35, comprising maintaining the ratio of aluminum and the total SCA in the range from about 0.5: 1 to 4: 1. 38. Способ по п.35, включающий введение в реактор газа с температурой точки росы на 1°C-10°C ниже, чем температура псевдоожиженного слоя, и снижение количества жидкого пропилена, присутствующего в реакторе.38. The method according to clause 35, comprising introducing into the reactor a gas with a dew point temperature of 1 ° C-10 ° C lower than the temperature of the fluidized bed, and reducing the amount of liquid propylene present in the reactor. 39. Способ по п.35, включающий увеличение времени пребывания для каталитической композиции.39. The method according to clause 35, including increasing the residence time for the catalytic composition. 40. Способ по п.35, по которому способ имеет норму выработки для полимерных частиц, способ включает поддержание норма выработки при снижении.40. The method according to clause 35, in which the method has a production rate for polymer particles, the method includes maintaining the production rate at a decrease. 41. Способ по п.35, включающий получение гомополимера полипропилена, имеющего содержание растворимых в ксилоле веществ приблизительно от 0,5 до 6 мас.%.41. The method according to clause 35, including obtaining a homopolymer of polypropylene having a content of soluble in xylene substances from about 0.5 to 6 wt.%. 42. Способ по п.35, включающий гашение с помощью каталитической композиции взаимодействия, когда температура псевдоожиженного слоя составляет приблизительно выше 100°C.42. The method according to clause 35, including quenching using the catalytic composition of the interaction, when the temperature of the fluidized bed is approximately above 100 ° C. 43. Способ по п.35, по которому пропиленсодержащий полимер содержит меньше, чем 3 млн-1 остаточного титана.43. The method according to clause 35, in which the propylene-containing polymer contains less than 3 million -1 residual titanium. 44. Способ полимеризации, включающий:44. The method of polymerization, including: введение газообразного пропилена, газообразного этилена и каталитической композиции в реактор-полимеризатор, каталитическая композиция содержит композицию прокатализатора Циглера-Натта, внутренний донор электронов в виде эфира ароматической дикарбоновой кислоты, алюминийсодержащий сокатализатор и агент для контроля за селективностью (SCA), включающий смесь ограничивающего активность агента и силановой композиции;introducing propylene gas, ethylene gas, and the catalyst composition into the polymerisation reactor, the catalyst composition contains a Ziegler-Natta procatalyst composition, an internal electron donor in the form of an aromatic dicarboxylic acid ester, an aluminum-containing cocatalyst, and a selectivity control agent (SCA) comprising a mixture of an activity limiting agent and silane composition; способ также включает поддержание соотношения алюминия и суммарного SCA в пределах от 0,5:1 до 4:1 иthe method also includes maintaining the ratio of aluminum and total SCA in the range from 0.5: 1 to 4: 1 and получение сополимера пропилена и этилена.obtaining a copolymer of propylene and ethylene. 45. Способ по п.44, включающий получение статистического сополимера пропилена и этилена, имеющего содержание этилена примерно свыше 4 мас.%.45. The method according to item 44, including obtaining a statistical copolymer of propylene and ethylene having an ethylene content of approximately more than 4 wt.%. 46. Способ по п.44, включающий снижение парциального давления газообразного пропилена в реакторе и формирование сферических частиц сополимера пропилена и этилена.46. The method according to item 44, including reducing the partial pressure of gaseous propylene in the reactor and the formation of spherical particles of a copolymer of propylene and ethylene. 47. Способ по п.46, по которому парциальное давление газообразного пропилена не снижают при получении полимера.47. The method according to item 46, in which the partial pressure of gaseous propylene is not reduced upon receipt of the polymer. 48. Способ полимеризации, включающий:48. The method of polymerization, including: введение пропилена и каталитической композиции в реактор-полимеризатор, каталитическая композиция содержит композицию прокатализатора Циглера-Натта, внутренний донор электронов в виде эфира ароматической дикарбоновой кислоты, алюминийсодержащий сокатализатор и агент для контроля за селективностью (SCA), включающий смесь силановой композиции и ограничивающего активность агента, выбираемого из группы, включающей алкиловый эфир C4-C30-алифатической кислоты, простой диэфир, (поли)(алкенгликолевый) эфир C4-C30-алифатической кислоты;introducing propylene and a catalytic composition into the polymerisation reactor, the catalytic composition contains a Ziegler-Natta procatalyst composition, an internal electron donor in the form of an aromatic dicarboxylic acid ester, an aluminum-containing cocatalyst, and a selectivity control agent (SCA), including a mixture of a silane composition and an activity limiting agent, selected from the group consisting of C 4 -C 30 aliphatic acid alkyl ester, diester, (poly) (alkene glycol) C 4 -C 30 aliphatic acid ester; поддержание соотношения алюминия и суммарного SCA в пределах от 0,5:1 до 50:1 иmaintaining the ratio of aluminum and total SCA in the range from 0.5: 1 to 50: 1 and получение пропиленсодержащего полимера. obtaining a propylene-containing polymer.
RU2010111142/04A 2007-08-24 2008-08-21 Self-limiting catalyst system with controlled aluminium to sca ratio and method RU2470947C2 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US95788807P 2007-08-24 2007-08-24
US60/957,888 2007-08-24
PCT/US2008/073882 WO2009029487A1 (en) 2007-08-24 2008-08-21 Self-limiting catalyst system with controlled aluminum rto sca ratio and method

Publications (2)

Publication Number Publication Date
RU2010111142A true RU2010111142A (en) 2011-09-27
RU2470947C2 RU2470947C2 (en) 2012-12-27

Family

ID=39768748

Family Applications (1)

Application Number Title Priority Date Filing Date
RU2010111142/04A RU2470947C2 (en) 2007-08-24 2008-08-21 Self-limiting catalyst system with controlled aluminium to sca ratio and method

Country Status (11)

Country Link
US (3) US10647788B2 (en)
EP (2) EP2185609B1 (en)
JP (1) JP5576281B2 (en)
KR (2) KR101576308B1 (en)
CN (3) CN101835812B (en)
BR (2) BRPI0815326B1 (en)
ES (1) ES2711342T3 (en)
MX (3) MX351199B (en)
PL (2) PL2185599T3 (en)
RU (1) RU2470947C2 (en)
WO (2) WO2009029487A1 (en)

Families Citing this family (42)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PL2185599T3 (en) 2007-08-24 2019-07-31 W.R. Grace & Co. - Conn Self-limiting catalyst system with controlled aluminium to sca ratio
KR101539286B1 (en) * 2008-05-21 2015-07-29 릴라이언스 인더스트리즈 리미티드 A catalyst system for polymeriazation of olefins
JP5628809B2 (en) * 2008-08-21 2014-11-19 ダウ グローバル テクノロジーズ エルエルシー Catalyst composition containing mixed selectivity control agent and polymerization method using the catalyst composition
ES2674584T3 (en) 2008-08-21 2018-07-02 W.R. Grace & Co. - Conn. Propylene impact copolymer with high melt index and corresponding method
PL2373702T3 (en) 2008-12-31 2018-07-31 W.R. Grace & Co.-Conn. Procatalyst composition with substituted 1,2-phenylene aromatic diester internal donor and method
WO2010078479A1 (en) 2008-12-31 2010-07-08 Dow Global Technologies Inc. Random propylene copolymer compositions, articles and process
CN101554595B (en) 2009-05-18 2011-02-02 中国石油化工股份有限公司 Catalyst support used for olefinic polymerization as well as preparation method and application thereof
MY158466A (en) 2009-12-02 2016-10-14 Grace W R & Co Three and four atom bridged dicarbonate compounds as internal donors in catalysts for polypropylene manufacture
SG181482A1 (en) 2009-12-02 2012-07-30 Dow Global Technologies Llc Two atom bridged dicarbonate compounds as internal donors in catalysts for polypropylene manufacture
SG181835A1 (en) * 2009-12-21 2012-08-30 Dow Global Technologies Llc Gas-phase polymerization process having multiple flow regimes
US20120116029A1 (en) * 2010-11-08 2012-05-10 Van Egmond Jan W Method for polymerizing polypropylene
US20120157645A1 (en) * 2010-12-21 2012-06-21 Linfeng Chen Procatalyst Composition with Alkoxypropyl Ester Internal Electron Donor and Polymer From Same
US20120157295A1 (en) 2010-12-21 2012-06-21 Linfeng Chen Process for Producing Procatalyst Composition with Alkoxyalkyl Ester Internal Electron Donor and Product
US9382342B2 (en) 2010-12-21 2016-07-05 W. R. Grace & Co.-Conn. Procatalyst composition with alkoxyalkyl 2-propenoate internal electron donor and polymer from same
US9382343B2 (en) 2010-12-21 2016-07-05 W. R. Grace & Co.-Conn. Procatalyst composition with alkoxypropyl ester internal electron donor and polymer from same
CN102174134B (en) * 2011-01-27 2013-07-24 大唐国际化工技术研究院有限公司 Catalyst composition for preparing polypropylene with high melt index, preparation method and application thereof
US10647790B2 (en) 2011-06-30 2020-05-12 W. R. Grace & Co.-Conn. Process for gas-phase polymerization having high bed bulk density
CN103044583B (en) * 2011-10-13 2015-10-28 中国石油化工股份有限公司 Olefin polymer and preparation method thereof
WO2013074087A1 (en) 2011-11-15 2013-05-23 Dow Global Technologies Llc Method for polymerizing polypropylene
EP2607384A1 (en) 2011-12-21 2013-06-26 Basell Poliolefine Italia S.r.l. Catalyst system for the polymerization of olefins
BR112015021953B1 (en) * 2013-03-14 2022-04-26 W. R. Grace & Co. -Conn Process for producing a propylene interpolymer
EP3036263B1 (en) * 2013-08-19 2023-10-11 Dow Global Technologies LLC Method for producing an ethylene based polymer in a polymerisation process using a self-limitng agent
TWI639626B (en) * 2013-09-30 2018-11-01 中國石油化工科技開發有限公司 Catalyst composition for olefin polymerization and application thereof
SG11201603245QA (en) * 2013-11-15 2016-05-30 Grace W R & Co Propylene-based polymer with reduced high-molecular weight portion
ES2687899T3 (en) * 2013-11-15 2018-10-29 Dow Global Technologies Llc Catalyst composition and polymerization method that uses it
US10093759B2 (en) 2013-11-21 2018-10-09 W. R. Grace & Co.-Conn. Producing high comonomer content propylene-based polymers
BR112016012137B1 (en) 2013-11-26 2022-04-05 W. R. Grace & Co.-Conn PROCESS TO PRODUCE A PROPYLENE IMPACT COPOLYMER
CN104774281A (en) * 2014-01-09 2015-07-15 金成豪 Catalyst composition used for olefin polymerization, and applications thereof
CN109843939B (en) 2016-08-30 2024-04-26 格雷斯公司 Polyolefin with low ash content and method for preparing same
RU2692246C1 (en) * 2017-06-15 2019-06-24 Индийская Нефтяная Корпорация Лимитэд External donor for olefin polymerization
CN109096421A (en) * 2017-06-21 2018-12-28 中国石油化工股份有限公司 A kind of catalyst and olefine polymerizing process for olefinic polymerization
CN109096424A (en) * 2017-06-21 2018-12-28 中国石油化工股份有限公司 A kind of catalyst and olefine polymerizing process for olefinic polymerization
CN109096418A (en) * 2017-06-21 2018-12-28 中国石油化工股份有限公司 A kind of catalyst and olefine polymerizing process for olefinic polymerization
CN109096420B (en) * 2017-06-21 2021-05-11 中国石油化工股份有限公司 Catalyst for olefin polymerization and olefin polymerization method
CN109096417A (en) * 2017-06-21 2018-12-28 中国石油化工股份有限公司 A kind of catalyst and olefine polymerizing process for olefinic polymerization
KR20200135776A (en) * 2018-02-07 2020-12-03 릴라이언스 인더스트리즈 리미티드 Ziegler-Natta catalyst system with self-extinguishing properties suitable for olefin polymerization
CN108409896B (en) * 2018-04-04 2021-02-05 朴蓝聚烯烃科技发展(上海)有限公司 Ziegler-natta catalyst compositions and uses thereof
WO2019228908A2 (en) 2018-05-28 2019-12-05 Borealis Ag Devices for a photovoltaic (pv) module
CN109517099B (en) * 2018-11-27 2021-07-30 山东鲁晶化工科技有限公司 External electron donor, olefin polymerization catalyst system and application thereof
CN113573806A (en) * 2019-03-15 2021-10-29 格雷斯公司 Catalyst system for producing olefin polymers without fine particles
WO2023018671A1 (en) * 2021-08-09 2023-02-16 W.R. Grace & Co.-Conn. Process for producing polyolefin granular resin with increased settled bulk density
WO2023056573A1 (en) * 2021-10-06 2023-04-13 W. R. Grace & Co.-Conn Gas-phase process for making polypropylene random copolymers

Family Cites Families (71)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IT1209255B (en) * 1980-08-13 1989-07-16 Montedison Spa CATALYSTS FOR THE POLYMERIZATION OF OLEFINE.
DE3247919A1 (en) * 1982-12-24 1984-06-28 Basf Ag, 6700 Ludwigshafen METHOD FOR PRODUCING HOMO AND COPOLYMERISATS FROM (ALPHA) MONOOLEFINES BY MEANS OF A ZIEGLER-NATTA CATALYST SYSTEM
US4746762A (en) 1985-01-17 1988-05-24 Mobil Oil Corporation Upgrading light olefins in a turbulent fluidized catalyst bed reactor
IN168393B (en) 1986-02-28 1991-03-23 Shell Oil Co
FI881337A (en) * 1987-03-23 1988-09-24 Idemitsu Petrochemical Co FOER FARING FRAMSTAELLNING AV POLYOLEFINER.
JPH0796573B2 (en) 1987-03-31 1995-10-18 出光石油化学株式会社 Method for producing propylene polymer
US5093415A (en) 1987-05-19 1992-03-03 Union Carbide Chemicals & Plastics Technology Corporation Process for producing stereoregular polymers having a narrow molecular weight distribution
US4882380A (en) 1987-07-07 1989-11-21 Union Carbide Chemicals And Plastics Company Inc. Process for the production of impact polypropylene copolymers
DE69019046T2 (en) 1989-03-02 1995-09-07 Mitsui Petrochemical Ind Process for the polymerization of olefins and catalyst for olefin polymerization.
JPH07119290B2 (en) 1989-11-28 1995-12-20 出光石油化学株式会社 Flexible polypropylene film and method for producing the same
FR2669639A1 (en) 1990-11-27 1992-05-29 Atochem COCATALYST FOR PROPYLENE POLYMERIZATION BASED ON SILANE AND MONOETHER.
US5432244A (en) 1990-12-12 1995-07-11 Union Carbide Chemicals & Plastics Technology Corporation Process for the production of polypropylene
US5218052A (en) 1991-02-04 1993-06-08 Amoco Corporation Olefin polymerization and copolymerization process
JP3443848B2 (en) 1992-11-04 2003-09-08 東ソー株式会社 Method for producing propylene block copolymer
TW300235B (en) * 1992-12-04 1997-03-11 Mitsui Petroleum Chemicals Ind
GB9300318D0 (en) 1993-01-08 1993-03-03 Oxford Analytical Instr Ltd Improvements relating to sample monitoring
US5462999A (en) * 1993-04-26 1995-10-31 Exxon Chemical Patents Inc. Process for polymerizing monomers in fluidized beds
TW354792B (en) 1993-08-13 1999-03-21 Mitsui Petrochemical Ind Olefin polymerization catalyst and process for preparing polypropylene and propylene block copolymer
IT1271420B (en) 1993-08-30 1997-05-28 Himont Inc POLYOLEFINIC COMPOSITIONS WITH A HIGH BALANCE OF RIGIDITY AND RESILIENCE
JP3508187B2 (en) 1993-11-10 2004-03-22 チッソ株式会社 Continuous production of propylene / ethylene block copolymer
JPH07149812A (en) 1993-12-02 1995-06-13 Tonen Corp Polymerization catalyst for alpha-olefin
US6133385A (en) 1994-04-06 2000-10-17 Fina Technology, Inc. Catalyst systems for improved stereoselectivity and broader molecular weight distribution in polymerization of olefins
JPH0812717A (en) * 1994-07-01 1996-01-16 Mitsubishi Chem Corp Production of propylene-ethylene block copolymer
US5529850A (en) 1994-07-05 1996-06-25 Montell North America Inc. Fibers produced from crystalline propylene polymers having high melt flow rate values and a narrow molecular weight distribution
JP3354729B2 (en) * 1994-11-28 2002-12-09 サンアロマー株式会社 Olefin polymerization catalyst and method for producing olefin polymer
IL117114A (en) 1995-02-21 2000-02-17 Montell North America Inc Components and catalysts for the polymerization ofolefins
IT1275573B (en) 1995-07-20 1997-08-07 Spherilene Spa PROCESS AND EQUIPMENT FOR GAS PHASE POMIMERIZATION OF ALPHA-OLEFINS
KR100430512B1 (en) 1995-08-31 2004-07-23 도요다 지도샤 가부시끼가이샤 Propylene-ethylene copolymer compositions and process for the production thereof
US6087459A (en) 1998-05-14 2000-07-11 Exxon Chemical Patents Inc. Polymeric materials formed using blends of electron donors
CN1138794C (en) 1998-05-14 2004-02-18 埃克森美孚化学专利公司 Polymeric materials formed using blends of electron donors
US6576697B1 (en) 1998-09-02 2003-06-10 Thayer A. Brown, Jr. Malleable high density polymer material
JP3182130B2 (en) 1999-01-25 2001-07-03 出光石油化学株式会社 Method for producing olefin polymer
KR20010043615A (en) 1999-03-15 2001-05-25 바셀 테크놀로지 컴퍼니 비.브이. Components and catalysts for the polymerization of olefins
JP4717219B2 (en) * 1999-04-15 2011-07-06 バセル テクノロジー カンパニー ビー.ブイ. Components and catalysts for olefin polymerization
BR0012952A (en) 1999-08-03 2002-04-30 Union Carbide Chem Plastic Method of detecting and correcting local defluidification and channeling in fluidized bed reactors for polymerization
US6391985B1 (en) 1999-10-21 2002-05-21 Union Carbide Chemicals & Plastics Technology Corporation High condensing mode polyolefin production under turbulent conditions in a fluidized bed
WO2001036502A1 (en) 1999-11-12 2001-05-25 Borealis Technology Oy Heterophasic copolymers
US6815512B2 (en) 2000-02-28 2004-11-09 Union Carbide Chemicals & Plastics Technology Corporation Polyolefin production using condensing mode in fluidized beds, with liquid phase enrichment and bed injection
US6460412B1 (en) * 2000-10-27 2002-10-08 Union Carbide Chemicals & Plastics Technology Corporation Detection of dynamic fluidized bed level in a fluidized bed polymerization reactor using ultrasonic waves or microwaves
US6825146B2 (en) 2001-05-29 2004-11-30 Union Carbide Chemicals & Plastics Technology Corporation Olefin polymerization catalyst compositions and method of preparation
EP1444276A1 (en) 2001-11-06 2004-08-11 Dow Global Technologies, Inc. Isotactic propylene copolymers, their preparation and use
US6906160B2 (en) 2001-11-06 2005-06-14 Dow Global Technologies Inc. Isotactic propylene copolymer fibers, their preparation and use
CN1310961C (en) 2002-01-03 2007-04-18 Bp北美公司 Gas phase olefin polymerizations using dual donor catalyst systems
CN1169845C (en) 2002-02-07 2004-10-06 中国石油化工股份有限公司 Solid catalyst component for olefine polymerization, catalyst with the component and its application
CA2488140A1 (en) * 2002-06-14 2003-12-24 Union Carbide Chemicals & Plastics Technology Corporation Catalyst composition and polymerization process using mixtures of selectivity control agents
KR101030711B1 (en) 2002-08-19 2011-04-26 우베 고산 가부시키가이샤 Catalysts for polymerization or copolymerization of ?-olefins, catalyst components thereof, and processes for polymerization of ?-olefins with the catalysts
US6753390B2 (en) 2002-09-04 2004-06-22 Univation Technologies, Llc Gas phase polymerization process
US6818711B2 (en) 2003-01-01 2004-11-16 Fina Technology, Inc. Polymerization of olefins using a ziegler-natta catalyst system having an external electron donor
US6759489B1 (en) 2003-05-20 2004-07-06 Eastern Petrochemical Co. Fluidized bed methods for making polymers
CN1856512B (en) 2003-09-23 2010-06-02 陶氏环球技术公司 Self limiting catalyst composition and propylene polymerization process
WO2005030815A1 (en) 2003-09-23 2005-04-07 Dow Global Technologies Inc. Self limiting catalyst composition and propylene polymerization process
WO2005035594A1 (en) 2003-09-23 2005-04-21 Union Carbide Chemicals & Plastics Technology Corporation Self-extiguishing catalyst compostion with monocarboxylic acid ester internal donor and propylene polymerization process
EP1548054B1 (en) 2003-12-26 2016-03-23 Japan Polypropylene Corporation Polypropylene-based resin composition and molded article thereof
JP3953466B2 (en) 2004-02-23 2007-08-08 日本ポリプロ株式会社 Polypropylene resin composition and molded body thereof
JP2005232395A (en) * 2004-02-23 2005-09-02 Toho Catalyst Co Ltd Olefin polymerization catalyst and method for producing olefin polymer by using the same
CN1938340A (en) 2004-04-07 2007-03-28 联合碳化化学及塑料技术公司 Olefin polymerization procatalyst compositions and method of preparation
US7226977B2 (en) 2004-04-19 2007-06-05 Sunoco, Inc. ( R&M) High melt flow rate thermoplastic polyolefins produced in-reactor
WO2006007093A1 (en) 2004-06-16 2006-01-19 Dow Global Technologies Inc. Apparatus and method for ziegler-natta research
CA2591823A1 (en) 2004-12-20 2006-06-29 Basell Poliolefine Italia S.R.L. Process and apparatus for the polymerization of propylene
EP1937348A2 (en) 2005-09-20 2008-07-02 Emerge Medsystems, LLC Embolic filter device and related systems and methods
CN101379097B (en) 2006-02-03 2011-08-03 日本聚丙烯公司 Propylene polymer, method for production of the propylene polymer, propylene polymer composition, and molded article manufactured from the composition
JP2007254671A (en) 2006-03-24 2007-10-04 Japan Polypropylene Corp Method for producing polypropylene
US20070270558A1 (en) 2006-05-16 2007-11-22 Paul Keith Scherrer Pulsing olefin polymerization fluidized-bed reactors
WO2007140019A1 (en) 2006-06-01 2007-12-06 Sunoco, Inc. (R & M) High crystallinity, high melt flow rate polypropylene
EP1935938A1 (en) 2006-12-18 2008-06-25 Borealis Technology Oy Improved high melt flow heterophasic polypropylene copolymers
PL2185599T3 (en) 2007-08-24 2019-07-31 W.R. Grace & Co. - Conn Self-limiting catalyst system with controlled aluminium to sca ratio
ES2674584T3 (en) 2008-08-21 2018-07-02 W.R. Grace & Co. - Conn. Propylene impact copolymer with high melt index and corresponding method
KR101510775B1 (en) 2008-11-24 2015-04-10 삼성전자주식회사 synchronous pulse plasma etching equipment
PL2373702T3 (en) * 2008-12-31 2018-07-31 W.R. Grace & Co.-Conn. Procatalyst composition with substituted 1,2-phenylene aromatic diester internal donor and method
WO2010078479A1 (en) 2008-12-31 2010-07-08 Dow Global Technologies Inc. Random propylene copolymer compositions, articles and process
BR112013015875B1 (en) * 2010-12-21 2020-10-20 W. R. Grace & Co. - Conn ziegler-natta polymerization process to produce a propylene-based polymer

Also Published As

Publication number Publication date
CN101835812B (en) 2013-10-02
JP2010537005A (en) 2010-12-02
RU2010111113A (en) 2011-09-27
KR20150140854A (en) 2015-12-16
EP2185599B1 (en) 2018-12-26
WO2009029486A2 (en) 2009-03-05
US8324327B2 (en) 2012-12-04
US20110152067A1 (en) 2011-06-23
CN101848946A (en) 2010-09-29
CN101835812A (en) 2010-09-15
EP2185609B1 (en) 2021-01-27
WO2009029486A3 (en) 2009-08-20
MX347799B (en) 2017-05-15
KR101716609B1 (en) 2017-03-14
BRPI0815326B1 (en) 2019-10-08
BRPI0815326A2 (en) 2015-02-10
BRPI0815290A2 (en) 2019-09-24
ES2711342T3 (en) 2019-05-03
RU2470947C2 (en) 2012-12-27
PL2185599T3 (en) 2019-07-31
US20110172377A1 (en) 2011-07-14
CN103467630A (en) 2013-12-25
US20190247818A1 (en) 2019-08-15
KR20100061502A (en) 2010-06-07
CN103467630B (en) 2016-08-10
WO2009029487A1 (en) 2009-03-05
US10647788B2 (en) 2020-05-12
EP2185609A2 (en) 2010-05-19
PL2185609T3 (en) 2021-06-14
WO2009029486A4 (en) 2009-11-05
CN101848946B (en) 2013-06-12
JP5576281B2 (en) 2014-08-20
MX2010002118A (en) 2010-08-09
WO2009029487A4 (en) 2009-06-04
MX351199B (en) 2017-10-05
EP2185599A1 (en) 2010-05-19
US10926234B2 (en) 2021-02-23
KR101576308B1 (en) 2015-12-09

Similar Documents

Publication Publication Date Title
RU2010111142A (en) SELF-RESTRICTED CATALYTIC SYSTEM WITH AN ADJUSTABLE RATIO OF ALUMINUM AND SCA AND METHOD
US5414063A (en) Process for the production of polypropylene
KR101716507B1 (en) Self-limiting catalyst composition with bidentate internal donor
US8178633B2 (en) Gas-phase polymerization process having multiple flow regimes
KR102416240B1 (en) Method for polymerizing polypropylene
JP2017048402A (en) Heterocyclic organic compounds as electron donors for polyolefin catalysts
EP2283048B1 (en) A catalyst system for polymerization of olefins
JPS60115610A (en) Production of block propylene copolymer
EP2958950B1 (en) An improved magnesium dichloride supported titanium catalyst composition for polyolefin polymerization
JPS63199207A (en) Polymerizable component of alpha-olefin and catalyst to stereoregular polymer having narrow molecular weight distribution
KR101954470B1 (en) Improved process for gas-phase polymerization having high polymer bed bulk density
JPH0796573B2 (en) Method for producing propylene polymer
KR20170015387A (en) Procatalyst for polymerization of olefins
KR101141846B1 (en) A method for preparation of a solid catalyst for polymerization of propylene
JPH0757769B2 (en) Solventless polymerization of olefins

Legal Events

Date Code Title Description
PC41 Official registration of the transfer of exclusive right

Effective date: 20140812